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Details

Stereochemistry ACHIRAL
Molecular Formula C24H38N6
Molecular Weight 410.5987
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMD-8664

SMILES

C(NCC1=NC=CC=C1)C2=CC=C(CN3CCCNCCNCCCNCC3)C=C2

InChI

InChIKey=CWJJHESJXJQCJA-UHFFFAOYSA-N
InChI=1S/C24H38N6/c1-2-13-29-24(5-1)20-28-19-22-6-8-23(9-7-22)21-30-17-4-12-26-15-14-25-10-3-11-27-16-18-30/h1-2,5-9,13,25-28H,3-4,10-12,14-21H2

HIDE SMILES / InChI

Molecular Formula C24H38N6
Molecular Weight 410.5987
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

AMD8664 (1-pyridin-2-yl-N-[4-(1,4,7-triazacyclotetradecan-4- ylmethyl)benzyl]methanamine) is an antagonist of CXCR4 receptor. It has therapeutic potential in the treatment of HIV. AMD8664 is an effective suppressor of choroidal neovascularization.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

mice: intravitreous injections 1 ul of AMD8664 (0.9 mM) or daily periocular injections of 5 ul AMD8664 (0.9 mM)
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:33:32 UTC 2023
Edited
by admin
on Sat Dec 16 08:33:32 UTC 2023
Record UNII
IMD9Z48ZTT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMD-8664
Code English
2-PYRIDINEMETHANAMINE, N-((4-(1,4,8,11-TETRAAZACYCLOTETRADEC-1-YLMETHYL)PHENYL)METHYL)-
Systematic Name English
AMD8664
Code English
Code System Code Type Description
CAS
185991-24-6
Created by admin on Sat Dec 16 08:33:32 UTC 2023 , Edited by admin on Sat Dec 16 08:33:32 UTC 2023
PRIMARY
PUBCHEM
483559
Created by admin on Sat Dec 16 08:33:32 UTC 2023 , Edited by admin on Sat Dec 16 08:33:32 UTC 2023
PRIMARY
FDA UNII
IMD9Z48ZTT
Created by admin on Sat Dec 16 08:33:32 UTC 2023 , Edited by admin on Sat Dec 16 08:33:32 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
TARGET ORGANISM->INHIBITOR
Related Record Type Details
ACTIVE MOIETY